I really like this: Manifesto for the post of National Director of Patient Insight with the NHS Commissioning Board The principles that will guide me if appointed: • I will press for power to be given to communities in all decisions about the commissioning of health services – for local, specialist and national services. • I will not align myself with the disingenuous euphemisms of government which claim to be putting patients at the ‘heart of’, ‘centre of’ and in the ‘driving seat of’ of services. I am in support of real power and influence for patients, carers and the public in the commissioning of services. • I will challenge the empty ritual of participation. I support communities having the real clout needed to affect the outcome of all commissioning processes in health care. • I am against participation without redistribution of power and the similar empty and frustrating processes currently promoted by the government in the name of public participation. • I bel
PPlog (Patient and Public Log) is an independent Service User watchdog/monitor for:
• social justice
* equality and human rights
• social care
• service user involvement and consultation
• disability and volunteer rights
And a base for blogs for Norfolk Disabled People Against the Cuts (DPAC).